A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457596



Internal ID22515477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51084736..51088435hg38UCSC Ensembl
chr12:51478519..51482218hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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